Job Responsibilities
- Support the management of the new Clinical Translational Catalyst initiative which provides funding and regulatory support for biotech companies to catalyze the translation of their pipeline from pre-clinical to clinical stage;
- Establish and maintain collaborative relationships with key stakeholders in the clinical translational path including Principal Investigators for Clinical Studies, Regulatory Professionals, Contract Research Organizations, Contract Manufacturing Organizations, and domain experts focusing in the fields of therapeutics and medical devices
Job Requirements
- Master degree in Pharmacology, Pharmaceutical Sciences, Pharmacy, Biomedical Sciences, Biochemistry, Biology, and related clinical science or medicine disciplines or equivalent;
- 5 to 8 years of experience, preferably in R&D of therapeutics or medical devices with focus in IND or PMA regulatory submissions (e.g. FDA, NMPA), GMP manufacturing and QC/QA